4-Chloro-1-methyl-1H-indazole is a chemical compound characterized by its indazole core, which is a bicyclic structure containing a five-membered ring fused to a six-membered ring. The presence of a chlorine atom at the 4-position and a methyl group at the 1-position contributes to its unique chemical properties. This compound is typically a solid at room temperature and is known for its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals. It may exhibit biological activity, including effects on various biological pathways, making it of interest in research. The molecular structure allows for various interactions, including hydrogen bonding and hydrophobic interactions, which can influence its solubility and reactivity. Additionally, the compound's stability and reactivity can be affected by the presence of the chlorine substituent, which can participate in electrophilic aromatic substitution reactions. Overall, 4-chloro-1-methyl-1H-indazole is a compound of interest in both synthetic and medicinal chemistry contexts.

4-chloro-1-methyl-1H-indazole

162502-53-6: 4-Chloro-1-methyl-1H-indazole is a chemical compound characterized by its indazole core, which is a bicyclic structure containing a five-membered ring fused to a six-membered ring. The presence of a chlorine atom at the 4-position and a methyl group at the 1-position contributes to its unique chemical properties. This compound is typically a solid at room temperature and is known for its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals. It may exhibit biological activity, including effects on various biological pathways, making it of interest in research. The molecular structure allows for various interactions, including hydrogen bonding and hydrophobic interactions, which can influence its solubility and reactivity. Additionally, the compound's stability and reactivity can be affected by the presence of the chlorine substituent, which can participate in electrophilic aromatic substitution reactions. Overall, 4-chloro-1-methyl-1H-indazole is a compound of interest in both synthetic and medicinal chemistry contexts.

CAS 162502-53-6

4-chloro-1-methyl-1H-indazole

1H-Indazole, 4-chloro-1-methyl-

Ref: IN-DA001T7C

4-Chloro-1-methyl-1H-indazole

Ref: 54-OR2244

4-Chloro-1-methyl-1H-indazole

Ref: 10-F067657